Classifications

• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
  • A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
  • A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms
  • A01N43/70—Diamino—1,3,5—triazines with only one oxygen, sulfur or halogen atom or only one cyano, thiocyano (—SCN), cyanato (—OCN) or azido (—N3) group directly attached to a ring carbon atom
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
  • A01N25/12—Powders or granules
  • A01N25/14—Powders or granules wettable
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
  • A01N33/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-oxygen bonds
  • A01N33/18—Nitro compounds
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
  • A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
  • A01N37/38—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
  • A01N37/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
  • A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
  • A01N41/04—Sulfonic acids; Derivatives thereof
  • A01N41/06—Sulfonic acid amides
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
  • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
  • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
  • A01N47/30—Derivatives containing the group >N—CO—N aryl or >N—CS—N—aryl
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
  • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
  • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
  • A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof

Definitions

• the present invention relates to phytopharmaceutical wettable powders comprising at least one active phytopharmaceutical substance which is solid at ambient temperature.
• wettable powder are meant pulverulent matters which, when mixed with water, provide stable suspensions.
• Phytopharmaceutical wettable powders comprising in powder form, in mixture, at least one phytopharmaceutical active substance solid at ambient temperature as well as an inert filler are already known.
• These phytopharmaceutical wettable powders are manufactured using so-called powder grinders, for instance those which are sold by the Company FORPLEX, and with which the phytopharmaceutical active solid substance is brought to a sufficient low degree of division or particle size; the drawback which is inherent to the use of these grinders comes from the fact that, for reasons of protection of the environment, it is necessary to filtrate the large volumes of air which are necessary for their running.
• a further drawback of the phytopharmaceutical wettable powders which are already known is that a certain number of active substances may be difficult to be ground, either because they are too hard, or because, while being solid, they show a plastic behaviour, or again because a softening occurs during grinding, or again because they have a melting point which is sufficiently low to be reached during grinding.
• the wettable powders which are already known and which are obtained by dry grinding of their various constitutive compounds may present some cutaneous toxicity with respect to the worker or the user, due to the fact that the finely divided active substances which are part of the powders may come in direct contact with the skin.
• the object of the invention is, above all, to overcome the drawbacks of the wettable powders of the prior art, i.e. essentially their toxicity as well as the pollution occuring during their manufacture.
• the phytopharmaceutical active substance which is solid at ambient temperature and which is selected from the group comprising:
• esters of the family of the parahydroxybenzonitriles of the group comprising bromoxynil octanoate, bromoxynil heptanoate, bromoxynil butyrate, ioxynil octanoate, ioxynil heptanoate, ioxynil butyrate,
• dinitroanilines of the group comprising butraline, pendimethaline, trifluraline, orizaline,
• the sulphonylureas of the group comprising especially chlorsulfuron is present within the wettable powder in the form a liquid phytopharmaceutical composition obtained by liquifying the said active substance by means of certain mineral and/or organic solvents, some of which are themselves active substances, and/or by means of surfactive agents and/or by mixture with another active substance proper to form with the phytopharmaceutical substance a liquid phase, especially an eutectic,
• the thus obtained wettable powder has a biological activity improved with respect to the biological activity of the phytopharmaceutical wettable powders according to the prior art.
• This improvement of the biological activity is consisting not only of a better selectivity and/or a better efficiency of the wettable powders according to the invention, but also in the enlargement of the possibilities of use of the said powders, especially from the point of view of the moment of their use, of the vegetative slade of the vegetables to be treated and of the various climatic conditions.
• the phytopharmaceutical wettable powder according to the invention which comprises at least one phytopharmaceutical active substance which is solid at ambient temperature and at least one pulverulent inert filler, is characterized by the fact that the constitutive particles of the filler constitute a support or carrier for the active substance comprised within a liquid composition, said active substance being selected from the group comprising:
• esters of the family of the parahydroxybenzonitriles of the group comprising bromoxynil octanoate, bromoxynil heptanoate, bromoxynil butyrate, ioxynil octanoate, ioxynil heptanoate, ioxynil butyrate,
• dinitroanilines of the group comprising butraline, pendimethaline, trifluraline, orizaline,
• the said liquid composition is obtained by liquifying the phytopharmaceutical active substance:
• a solvent selected from the group comprising aliphatic, aromatic, cycloaliphatic mineral oils, solvents of petroleum origin of the alkylaromatic type, plant oils, dimethylformamide, dimethylsulphoxide, dimethylacetamide, N-methylpyrrolidone, dimethylimidazolinone, hexamethylene-phosphotriamide, cyclohexanone, acetophenone, alcohol diacetone, butylbenzylphthalate, dialkylphthalates, short alcohols with a chain in C 1 to C 8 and their oxyethylenated and/or oxypropylenated derivatives, ethyleneglycol, propyleneglycol, and the solvents on the basis of alkylbenzene and alkylnaphthalene, in which the alkyl chain comprises from 1 to 8 carbon atoms, and/or
• liquid active substance selected from the group comprising, on the one hand, the phenoxyacids, especially 4- and 3-chlorophenoxyacetic acid, 2.4-D, MCPA, mecoprop and dichlorprop as well as their dextrogyre isomers, in the form of esters of the group comprising those of butyglycol, 2-ethylhexanol, isooctanol and of the alcohols in C 8 , on the other hand the fluazifop-butyl, metolachlor, pretilachlor, sethoxydime, tebutame, and/or
• a surfactive agent selected from the group comprising:
• non-ionic surfactive agents obtained by reaction of ethylene and/or propylene oxide on fatty alcohols, alkylphenols, tristyrylphenols, fatty amides, fatty amines,
• anionic surfactive agents which are the sulphonated, sulphated or phosphorated derivatives of the above-mentioned non-ionic surfactive agents, possibly neutralized by aliphatic amines, alkanolamines or sodium or potassium hydroxide,
• calcium dodecylbenzenesulphonate calcium alkylbenzenesulphonates having a alkyl chain in C 12 to C 18 , sodium or calcium alkylnaphthalenesulphonates, sodium, calcium or ammonium lignosulphonates, formol/cresol/ betanaphtholsulphonate condensates and/or
• bromoxynil octanoate with bromoxynil heptanoate, the proportions being respectively 50% and 50% by weight, the melting point being 26° C.
• alkylbenzene and alkylnaphtalene may be selected from those known under the trademarks SHELL SOL R®, SOLVESSO 200® and NAPHTA® commercialized respectively by the Companies SHELL, ESSO or EXXON and TOTAL.
• the solvent and/or the liquid active substance selected for liquifying are present in an amount of at most 50% by weight and preferably of at most 25% by weight, the surfactive agent being present in a proportion of at most 20% by weight and preferably in a proportion of 5 to 10% by weight with respect to the total weight of the liquid composition.
• the process for the preparation of the phytopharmaceutical wettable powder according to the invention is characterized by the fact that there is prepared a liquid composition by liquifying at least one phytopharmaceutical active solid substance of the above-identified group, by means of a solvent and/or by means of a liquid active substance and/or by means of a surfactive agent and/or by formation of an eutectic with another solid active substance of the group hereabove defined, the said liquid composition being applied on the constitutive particles of an inert pulverulent filler.
• a special advantage of the process according to the invention is that the active substance(s) are distributed in a homogeneous manner within the said powder, which is especially advantageous when, in the event that several active substances are used, one of the said substances is present in an amount very lower than that of the other active substances.
• These powders comprise from 1 to 50% by weight and preferably from 10 to 25% by weight of at least one of the above-mentioned phytopharmaceutical active substances.
• the pulverulent inert filler which constitutes the carrier of the phytopharmaceutical active substance comprised within the said liquid composition can be selected from the group comprising silica and clays.
• Illustrative examples of carriers are those known under the trademarks TIX-O-SIL 38® and ARGIREC B 22®, respectively commericialized by RHONE-POULENC and BLANC MINERAUX DE PARIS.
• the phytopharmaceutical wettable powder according to the invention comprises from 30 to 95% by weight of at least one pulverulent carrier with respect to the total weight.
• the above-mentioned liquid composition is slowly poured on the pulverulent inert filler which constitutes an absorbent carrier which is stirred in a powder mixer.
• the powder mixers which are adapted to be used in the process or method according to the invention may consist of horizontal drums equipped with paddles, by belt-, impeller-, screw-, discs- or sockets-mixers, or by any other device allowing the mixture of powders.
• the devices known under the trademarks MYERS®, VIDAX®, SEVIN®, LODIGE®, TURBOSPHERE® can be used.
• the output of the liquid composition which is poured or sprayed on the inert filler, the speed of stirring of the carrier as well as the respective proportions of the liquid composition and of the filler are adjusted in such a way that there is obtained a homogeneous wettable powder which flows easily.
• the homogeneity of the wettable powder can be evaluated visually or measured on samples.
• the wettable powder thus obtained contains few or no agglomerates and the walls of the mixing device are clean.
• sand wettable powder wetting agents, dispersing agents and surfactive agents for example, it is possible to add by spraying a liquid surfactive agent playing an anti-dust role or by dusting of a surfactive agent which is solid; it is also possible to add to the said wettable powder further active substances in the form of powder of the group comprising amino-triazole and the sodium, potassium and/or magnesium salts of phenoxyacids such as mecoprop, these active substances having to be soluble in water at the dose of use of the final wettable powder on the plants; it is also possible to add a "conventional" wettable powder, that is to say a wettable powder obtained by dry grinding of its various constituents.
• a particular advantage of the process of preparation according to the invention of the phytopharmaceutical wettable powder is that it does not necessitate any drying, the consequence being a simplification and a reduction of the cost of the wettable powder.
• a wettable powder according to the invention on the basis of bromoxynil octanoate is prepared, the proportion of the said active substance within the wettable powder being 20% by weight.
• the emulsifying agents known under the trademark GALORYL EM consist of non-ionic surface active agents of the fatty alcohol type or of the type corresponding to polyethoxylated castor oil, these agents being possibly used together with calcium dodecylbenzenesulfonate.
• the solubilization of the bromoxynil octanoate can be improved by a light heating to 40°-50° C.
• a homogenous liquid is obtained.
• a mixing device which may be one of those sold by the Company MYERS, on 41 parts by weight of a silica known under the trademark TIX-O-SIL 38®; inside the said mixing device, 1 part by weight of a wetting agent known under the trademark GALORYL MT 41182 ® (non-ionic wetting agent on the basis of alkylarylsulfonates and lignosulfonates) and 8 parts by weight of a dispersing agent known under the trademark GALORYL DT 201® (a polymer of hydroxynaphthalene sodium sulfonate and of methylphenol); are added.
• GALORYL MT 41182 non-ionic wetting agent on the basis of alkylarylsulfonates and lignosulfonates
• GALORYL DT 201® a polymer of hydroxynaphthalene sodium sulfonate and of methylphenol
• the mixture is homogenized.
• a beige colour powder having a particle size lower than 250 ⁇ m (standard AFNOR N° 25) is obtained; the wettability of the said powder in hard water (according to the standard OMS, introduction of 1 gram of powder into 100 ml of water) is from 30 to 40 seconds at most and its suspensivity (type FISHER, hard water OMS, introduction of 10 grams of powder into 1 liter of water, 15 turns-up and then standing during 30 minutes) is 80% at least.
• This powder has the following centesimal composition:
• a wettage powder according to the invention is prepared on the basis of 10% by weight of bromoxynil in the form of octanoate and 10% by weight of bromoxynil in the form of heptanoate.
• the solubilization of the bromoxynil octanoate and of the bromoxynil heptanoate can be improved by a light heating to 40°-50° C.
• the thus obtained solution is applied inside a mixer which may be selected among those commercialized by the Company MYERS, onto 41 parts by weight of a silica of the trademark TIX-O-SIL 38®; inside the said mixture there are added 1 part by weight of wetting agent known under the trademark GALORYL MT 41182® and 8 parts by weight of a dispersing agent known under the trademark GALORYL DT201®.
• the mixture is homogenized.
• a beige colour powder having a particle size lower than 250 ⁇ m (standard AFNOR N° 25) is obtained, the wettability of the said powder in hard water (according to the standard OMS, introduction of 1 gram of powder into 100 ml of water) is from 30 to 40 seconds at most and its suspensivity (type FISHER, hard water OMS, introduction of 10 grams of powder into 1 liter of water, 15 turns-up and then standing during 30 minutes) is 80% at least.
• the thus obtained powder has the following centesimal composition:
• powder A a wettable powder corresponding to the prior art, called powder A, whose composition is indicated hereafter and which is different from the powder according to the invention by the fact that it does not comprise an intermediate liquid composition obtained by means of a solvent, the solvent being substituted by an equivalent quantity of silica.
• the phytopharmaceutical active substance of powder A corresponding to the prior art is consisting of bromoxynil octanoate whose content in active substance is 65.3% by weight.
• Powder A thus obtained has the following centisomal composition:
• a wettable powder according to the invention is prepared on basis of 6% by weight of ioxynil in the form of octanoate, 6% by weight of ioxynil in the form of heptanoate and 18% by weight of dextrogyre mecoprop (MCPP) in the form of butylglycol ester (BG).
• MCPP dextrogyre mecoprop
• the solubilization of the active substances can be improved by a light heating to 40°-50° C.
• a homogeneous transparent liquid is obtained.
• a mixer which may be one of those commercialized by the Company MYERS, on 41 parts by weight of a silica of the trademark TIX-O-SIL 38®; there is added inside the said mixer 1 part by weight of a wetting agent known under the trademark GALORYL MT 41182® and 8 parts by weight of a dispersing agent known under the trademark GALORYL DT 201®.
• the mixture is homogenized inside the said mixer.
• the thus obtained powder has the following centesimal composition:
• a wettable powder according to the invention on the basis of 25% by weight of butraline is prepared.
• the solubilization of butraline can be promoted by a light heating to 45°-50° C.
• the mixture is homogenized inside the mixer.
• the thus obtained powder has the following centesimal composition:
• a wettable powder according to the invention on the basis of 13% by weight of bromoxynil in the form of octanoate and 26% by weight of dextrogyre mecoprop in the form of magnesium salt is prepared.
• the preparation of the said wettable powder according to the invention is consisting in the mixture of two wettable powders which are prepared independently of one another.
• powder B is on the basis of 75% by weight of dextrogyre mecoprop in the form of magnesium salt.
• Powder B is prepared by mixing, inside a powder mixer of the trademark LODIGE, 93.75 parts by weight of dextrogyre mecoprop in the form of magnesium salt having a content in active substance of 80%, 1 part by weight of a dispersing agent of the trademark GALORYL MT 41182®, 2 parts of a dispersing agent of the trademark GALORYL DT 201® and 3.25 parts by weight of a silica of the trademark TIX-O-SIL 38®.
• the thus obtained powder B has the following centesimal composition:
• the wettable powder on the basis of bromoxynil octanoate and of dextrogyre mecoprop in the form of magnesium salt is obtained by mixing 65 parts by weight of the wettable powder according to example 1, 34.6 parts by weight of powder B and 0.4 part by weight of a silica of the trademark TIX-O-SIL 38®; its centisemal composition is as follows:
• the products I and II are commercial products according to the prior art whose biological activities are well known with respect to corn on the level of their phytotoxicity, as well as on the level of herbicidal efficiency with respect to usual weeds in corn crops, these plants which are difficult to be destroyed being Chenopodes and Amarantes.
• the useful and necessary doses at which the said products have been applied are determined as a function of an efficiency level of at least 80% of destruction and, if possible, close to 90% as a function of the selectivity.
• the average dose is 600 grams of active substance/hectare within a practical range from 450 to 750 grams of active substance/hectare,
• the average useful dose is 350 grams of active substance/hectare in order to be close to acceptable efficiency levels
• the average useful dose is 450 grams of active substance/hectare in order to be close to acceptable efficiency levels
• the average useful dose is 600 grams of active substance/hectare.
• Each treatment is applied on two elementary experimental plots A and B located in three different fields.
• the application of the products is carried out when the corn is at the stage from 4 to 6 leaves, and when the weeds are between the stages of 2 cotyledon leaves and from 4 to 6 true leaves.
• the application of the different products is carried out by normal spray at a rate of 250 liters of spray-mixture per hectare.
• Each product (I to V) has been applied at the rate of 2 doses of active substance/hectare; the underlined dose in Table II corresponds to recommended dose of use.
• the phytotoxicity on corn the phytotoxicity being appreciated as an average percentage of necrosed leave surface
• the wettable powders according to the invention while having a general effect clearly better than concentrated suspension and emulsifiable concentrate, are hardly more phytotoxic as the conventional wettable powder and are significantly more efficient than the latter while having a content in active substance/hectare clearly lower.
• the wettable powder according to the invention shows a phytotoxicity against corn better or comparable to that of a conventional wettable powder, the dose of active substance being twice lower per hectare, this is an improvement from the economical point of view as well as from the point of view of environmental protection, a better advantage being taken of the active substance. Furthermore, the wettable powder according to the invention provides a very great security for corn in case of overdose with respect to the existing formulations of the emulsifiable concentrate type, of the aqueous solution type, or of the concentrated suspension type.
• a wettable powder according to the invention and a conventional wettable powder are prepared from a triazine, namely ametryne.
• Crushing is carried out in a grinder equipped with a 1-2 mm grid.
• a beige colour powder is obtained; its particle size is lower than 200 ⁇ m and its wettability in hard water OMS, introduction of 1 g of powder into 100 ml of water, is from 30 seconds at most.
• An intimate mixing is performed in a grinder equipped with a 0.5 mm grid.
• the thus obtained beige colour powder has a particle size lower than 100 ⁇ m and a wettability in hard water OMS, introduction of 1 g of powder in 100 ml of water, of 1 minute at most.
• the two powders have been applied at the rate of 1000, 2000 and 3000 g/ha of active substance by spraying a spray-mixture at the dose of 500 l/ha on earthenwares (terrines) of 10 ⁇ 20 cm in which dicotyledon weed species are sawn.
• the wettable powder according to the invention shows a very clear superiority, even in pre-emergence, with respect to the conventional wettable powder.
• the two powders have been applied at the rate of 1000, 2000 and 3000 g/ha of active substance by spraying of a spray-mixture at the dose of 500 l/ha, on earthenwares of 10 ⁇ 20 cm in which different gramineous weed species have been sawn 15 to 20 days before.
• the wettable powder according to the invention shows a very clear superiority with respect to a conventional wettable powder.
• Powder M wettable powder identical to Powder K, except the fact that the solvent of petroleum origin is replaced by silica, this Powder M being prepared as indicated hereafter.
• the mixture is homogenized and crushed in a grinder equipped with a 1 mm grid.
• the thus obtained yellow powder of particle size lower than 200 ⁇ m has a wettability in hard water OMS (introduction of 1 g of powder in 100 ml of water) from 2 to 3 minutes.
• the mixture is homogenized inside the mixer and crushed in a grinder equipped with a 1 mm grid.
• a yellow powder of particle size lower than 200 ⁇ m is obtained; its wettability in hard water OMS (introduction of 1 g of powder in 100 ml of water) is at most 1 minute.
• Each one of powders K, L and M has been applied at the rate of 1000 and 3000 g/ha of active substance (butraline) by spraying of a spray-mixture at the dose of 500 l/ha on earthenwares of 10 ⁇ 20 cm in which different gramineous and dicotyledonous weed species have been sawn.
• active substance butraline

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• Life Sciences & Earth Sciences (AREA)
• Health & Medical Sciences (AREA)
• General Health & Medical Sciences (AREA)
• Dentistry (AREA)
• Plant Pathology (AREA)
• Engineering & Computer Science (AREA)
• Pest Control & Pesticides (AREA)
• Agronomy & Crop Science (AREA)
• Wood Science & Technology (AREA)
• Zoology (AREA)
• Environmental Sciences (AREA)
• Toxicology (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Medicines Containing Plant Substances (AREA)

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Citations (6)

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• 1991
  • 1991-06-20 FR FR9107592A patent/FR2677849B1/fr not_active Expired - Lifetime
• 1992
  • 1992-06-19 CA CA002071728A patent/CA2071728C/en not_active Expired - Lifetime
  • 1992-06-19 HU HU9202076A patent/HU212609B/hu unknown
  • 1992-06-19 ZA ZA924539A patent/ZA924539B/xx unknown
  • 1992-06-19 IT ITMI921514A patent/IT1254979B/it active IP Right Grant
  • 1992-06-19 AU AU18436/92A patent/AU657760B2/en not_active Expired
  • 1992-06-19 DE DE69226685T patent/DE69226685T2/de not_active Expired - Lifetime
  • 1992-06-19 EP EP92401731A patent/EP0522906B1/de not_active Expired - Lifetime
  • 1992-06-19 NL NL9201087A patent/NL9201087A/nl not_active Application Discontinuation
  • 1992-06-19 GR GR920100274A patent/GR1002611B/el not_active IP Right Cessation
  • 1992-06-19 AT AT92401731T patent/ATE169795T1/de active
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